EP1088567B1 - Drug delivery devices - Google Patents

Drug delivery devices Download PDF

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Publication number
EP1088567B1
EP1088567B1 EP01100963A EP01100963A EP1088567B1 EP 1088567 B1 EP1088567 B1 EP 1088567B1 EP 01100963 A EP01100963 A EP 01100963A EP 01100963 A EP01100963 A EP 01100963A EP 1088567 B1 EP1088567 B1 EP 1088567B1
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EP
European Patent Office
Prior art keywords
valve
metering
valve stem
container
valve member
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP01100963A
Other languages
German (de)
French (fr)
Other versions
EP1088567A2 (en
EP1088567A3 (en
Inventor
Richard John Warby
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Consort Medical PLC
Original Assignee
Bespak PLC
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Filing date
Publication date
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Priority claimed from GBGB9803780.7A external-priority patent/GB9803780D0/en
Priority claimed from GBGB9808804.0A external-priority patent/GB9808804D0/en
Priority claimed from GBGB9814717.6A external-priority patent/GB9814717D0/en
Application filed by Bespak PLC filed Critical Bespak PLC
Publication of EP1088567A2 publication Critical patent/EP1088567A2/en
Publication of EP1088567A3 publication Critical patent/EP1088567A3/en
Application granted granted Critical
Publication of EP1088567B1 publication Critical patent/EP1088567B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D83/00Containers or packages with special means for dispensing contents
    • B65D83/14Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant
    • B65D83/44Valves specially adapted therefor; Regulating devices
    • B65D83/52Valves specially adapted therefor; Regulating devices for metering
    • B65D83/54Metering valves ; Metering valve assemblies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M15/00Inhalators
    • A61M15/009Inhalators using medicine packages with incorporated spraying means, e.g. aerosol cans
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/62Plasma-deposition of organic layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D83/00Containers or packages with special means for dispensing contents
    • B65D83/14Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant
    • B65D83/75Aerosol containers not provided for in groups B65D83/16 - B65D83/74
    • B65D83/752Aerosol containers not provided for in groups B65D83/16 - B65D83/74 characterised by the use of specific products or propellants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/02General characteristics of the apparatus characterised by a particular materials
    • A61M2205/0222Materials for reducing friction
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D5/00Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
    • B05D5/08Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain an anti-friction or anti-adhesive surface
    • B05D5/083Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain an anti-friction or anti-adhesive surface involving the use of fluoropolymers

Definitions

  • This invention relates to improvements in drug delivery devices and particularly those for dispensing a metered dose of medicament.
  • the document WO-A-96/28367 is regarded as the closest prior art.
  • an aerosol stream from a pressurised dispensing container is fired towards a patient or user of the inhaler into an air flow.
  • the air flow is created by a user inhaling through a mouthpiece of the inhaler and the medicament is released into this air flow at a point between the air inlet holes and the mouthpiece.
  • Conventional metering valves for use with pressurised dispensing containers comprise a valve stem coaxially slidable within a valve member defining an annular metering chamber, and outer and inner annular seals operative between the respective outer and inner ends of the valve stem and the valve member to seal the metering chamber therebetween.
  • the valve stem is hollow whereby in a non-dispensing position of the valve stem, the metering chamber is connected to the container and charged with product therefrom.
  • the valve stem is movable against the action of a spring to a dispensing position wherein the metering chamber is isolated from the container and vented to atmosphere for the discharge of product.
  • Other drug delivery devices include apparatus in which capsules containing a powdered medicament are mechanically opened at a dispensing station where inhaled air subsequently entrains the powder, which is then dispensed through a mouthpiece.
  • a problem with all such drug delivery devices is that deposition of the medicament, or a solid component from a suspension of a particulate product in a liquid propellant, on the internal surfaces and other components of the devices occurs after a number of operation cycles and/or storage. This can lead to reduced efficiency of operation of the device and of the resulting treatment in that deposition of the product reduces the amount of active drug available to be dispensed.
  • a metering valve (110) for use with a pressurised dispensing container, the valve comprising a valve stem (111) co-axially slidable within a valve member (112), said valve member and valve stem defining an annular metering chamber (113), the metering valve further comprising outer and inner annular seals (117.118) operative between respective outer and inner ends of the valve member and the valve stem to seal the annular metering chamber therebetween, characterised in that the metering valve (110) comprises a layer of a clod plasma polymerised siloxane bonded to at least a portion of an internal surface of the valve member (112).
  • an inhaler 10 for a product such as a medicament comprises a housing 11 for receiving a pressurised dispensing container 12 of a medicament and a mouthpiece 14 for insertion into the mouth of a user of the inhaler 10.
  • the container housing 11 is generally cylindrical and open at its upper end.
  • a lower wall 15 of the housing 11 includes an annular socket 16 for receiving the tubular valve stem 17 of the container 12.
  • the socket 16 communicates via a duct 18 ending in an orifice 19 with the mouthpiece 14.
  • the lower wall 15 also has holes 20 for allowing air to flow through the container housing 11 into the mouthpiece 14.
  • the mouthpiece 14 may be generally circular or shaped to fit the mouth and is connected to or forms a part of the housing 11.
  • a patient or user holds the inhaler 10, usually in one hand, and apples his mouth to the mouth piece 14.
  • the user then inhales through the mouthpiece 14 and this creates an airflow through the cylindrical housing 11, from its open end around the dispensing container 12, through the holes 20 and into the mouthpiece 14.
  • the container 12 is depressed downwardly onto its stem 17 to release a dose of medicament from the container 12.
  • the dose of medicament is projected by the pressure in the container 12 via the duct 18 and through the orifice 19. It then mixes with the airflow through the mouthpiece 14 and is hence inhaled by the user.
  • the components are plastic mouldings, which gives rise to the deposition problems described above.
  • the particular problem areas in devices such as inhalers are the internal surfaces 21 of the mouthpiece 14, the internal surfaces 22 of the duct 18 and the walls 23 defining the orifice 19.
  • the diameter of at least a part of the duct 18 can be as little as 0.5mm and so any deposition on its internal surfaces 22 could lead to not only the problem of a reduction in active drug components being available, but also dispensing difficulties.
  • the metering valve 110 illustrated in Figure 2 is another type of drug delivery device or dispenser, and includes a valve stem 111 which protrudes from and is axially slidable within a valve member 112, the valve member 112 and valve stem 111 defining therebetween an annular metering chamber 113.
  • the valve member 112 is located within a valve body 114 which is positioned in a pressurised container (not shown) containing a product to be dispensed.
  • the metering valve 110 is held in position with respect to the container by means of a ferrule 115 crimped to the top of the container and sealing being provided between the valve body 114 and container by an annular gasket 116.
  • An outer seal 117 and an inner seal 118 of an elastomeric material extend radially between the valve stem 111 and the valve member 112.
  • the outer seal 117 is radially compressed between the valve member 112 and valve stem 111 so as to provide positive sealing contact, the compression being achieved by using a seal which provides an interference fit on the valve stem 111 and/or by the crimping of the ferrule 115 onto the pressurised container during assembly.
  • the valve stem 111 has an end 119 which protrudes from the valve member 112 and ferrule 115 which is a hollow tube and which is closed off by flange 120 which is located within the metering chamber 113.
  • the hollow end 119 of valve stem 111 includes a discharge port 121 extending radially through the side wall of the valve stem 111.
  • the valve stem 111 further has an intermediate section 122, which is also hollow and defining a central passage and which has a pair of spaced radial ports 123, 124 which are interconnected through a central cavity.
  • a spring 125 extends between a second flange 126, separating the intermediate section 122 of the valve stem 111 and an inner end 127 of the valve stem 111, and an end of the valve body 114 to bias the valve stem 111 in a non-dispensing position in which the first flange 120 is held in sealing contact with the outer seal 117.
  • the second flange 126 is located outside the valve member 112, but within the valve body 114.
  • the metering chamber 113 is sealed from the atmosphere by the outer seal 117, and from the pressurised container to which the valve 110 is attached by the inner seal 118.
  • radial ports 123, 124, together with the central cavity in the intermediate section 122 of the valve member 111 connect the metering chamber 113 with the container so that in this non-dispensing condition the metering member 113 will be charged with product to be dispensed.
  • the radial port 124 Upon depression of the valve stem 111 relative to the valve member 112 so that it moves inwardly into the container, the radial port 124 is closed off as it passes through the inner seal 118, thereby isolating the metering chamber 113 from the contents of the pressurised container.
  • the discharge port 121 Upon further movement of the valve stem 111 in the same direction to a dispensing position the discharge port 121 passes through the outer seal 117 into communication with the metering chamber 113. In this dispensing position the product in the metering chamber 113 is free to be discharged to the atmosphere via the discharge port 121 and the cavity in the hollow end 119 of the valve stem 111.
  • valve stem 111 When the valve stem 111 is released, the biasing of the return spring 125 causes the valve stem 111 to return to its original position. As a result the metering chamber 113 becomes recharged in readiness for further dispensing operations.
  • the component parts of the metering valve are generally formed as single mouldings from material such as acetal, polyester or nylon which are prone to the deposition problems described above.
  • material such as acetal, polyester or nylon which are prone to the deposition problems described above.
  • a separate liner of a material such as a fluoropolymer, ceramic or glass to line a portion of the area in which deposition problems occurs, this requires the re-design or modification of mouldings and mould tools so that the components can accommodate.such liners.
  • the component parts of the drug dispensing devices are made by conventional tooling and moulds from the traditional materials listed above. They are then subjected to a cold plasma polymerisation treatment of one or more monomers which is a "hydrophobic" treatment which creates a very thin layer of the plasma polymer on the surface of the component parts which significantly reduces the deposition of active drugs on the relevant surfaces due to factors such as anti-frictional and waterproof characteristics and low surface energy.
  • the preferred monomers to use in this process are siloxanes, such as dimethyl siloxane, to give a layer of plasma polymerised dimethylsiloxane.
  • thermoplastic materials such as polybutyrene terephthalate (PBT), nylon, acetile and tetrabutyrene terephthalate (TBT) can be treated without fear of thermal damage.
  • the treatment is a vacuum procedure in which the components are placed inside a chamber which is evacuated to less than 0.005 Torr.
  • One or more monomers are introduced to the chamber at a controlled rate and a 13.56 MHZ r.f. signal is applied to an external antenna.
  • the plasma is ignited within the chamber and maintained for a given time at the preselected power setting.
  • the plasma is extinguished, the chamber flushed and the products retrieved.
  • a thin layer for example 0.005 to 0.5 microns
  • the valve member 112 alone may be treated.
  • additional benefits can be achieved in treating some or all of the other plastic and rubber parts of the valve, including the valve body 114 and the seals 116, 117 and 118.
  • Treatment of the seals 117 and 118 has the additional benefit that fiction between the seals 117 and 118 and valve stem 111 is reduced resulting in easier operation of the device.
  • the level of friction between the valve stem 111 and seals 117 and 118 may be further reduced by treatment of the valve stem 111 itself.
  • Such treatment reduces or eliminates the need for silicone emulsions or oils to be applied to the seals 117 and 118 and valve stem 111.
  • Treatment of the seals 116, 117 and 118 also has the benefits of reducing levels of extractibles where the seals are manufactured from elastomeric materials, reducing the permeability of the seals to the propellant in the pressurised dispensing container and reducing the levels of absorption of product onto the surfaces of the seals.
  • the method can also be used to treat components of many other delivery devices including nasal pumps, non-pressurised actuators, breath actuated inhaler devices and breath co-ordinating devices and so on.

Description

  • This invention relates to improvements in drug delivery devices and particularly those for dispensing a metered dose of medicament. The document WO-A-96/28367 is regarded as the closest prior art.
  • In metered dose inhalers, an aerosol stream from a pressurised dispensing container is fired towards a patient or user of the inhaler into an air flow. The air flow is created by a user inhaling through a mouthpiece of the inhaler and the medicament is released into this air flow at a point between the air inlet holes and the mouthpiece.
  • Conventional metering valves for use with pressurised dispensing containers comprise a valve stem coaxially slidable within a valve member defining an annular metering chamber, and outer and inner annular seals operative between the respective outer and inner ends of the valve stem and the valve member to seal the metering chamber therebetween. The valve stem is hollow whereby in a non-dispensing position of the valve stem, the metering chamber is connected to the container and charged with product therefrom. The valve stem is movable against the action of a spring to a dispensing position wherein the metering chamber is isolated from the container and vented to atmosphere for the discharge of product.
  • Other drug delivery devices include apparatus in which capsules containing a powdered medicament are mechanically opened at a dispensing station where inhaled air subsequently entrains the powder, which is then dispensed through a mouthpiece.
  • A problem with all such drug delivery devices is that deposition of the medicament, or a solid component from a suspension of a particulate product in a liquid propellant, on the internal surfaces and other components of the devices occurs after a number of operation cycles and/or storage. This can lead to reduced efficiency of operation of the device and of the resulting treatment in that deposition of the product reduces the amount of active drug available to be dispensed.
  • Some prior art devices rely on the dispenser being shaken in an attempt to dislodge the deposited particles as a result of the movement of a liquid propellant and product mixture. However, whilst this remedy is effective within the body of the container itself, it is not effective for particles deposited on the inner surfaces of the metering chamber. As the size of the chamber is significantly smaller, the restricted flow of fluid in the metering chamber (caused by the tortuosity of the flow path through the chamber) means that the fluid in the metering chamber does not move with enough energy to adequately remove the deposited particles.
  • One solution is proposed in our pending application GB 97211684.0 in which a liner of a material such as fluoropolymer, ceramic or glass is included to line a portion of the wall of a metering chamber in a metering valve. Although this solves the problem of deposition in these types of dispensers, it does require the re-design or modification of moldings and mould tools for producing the valve members to allow for the insertion of the liner.
  • It is an object of the present invention to provide drug delivery devices in general in which the deposition of the product and active drug component is minimised.
  • According to the invention there is provided a metering valve (110) for use with a pressurised dispensing container, the valve comprising a valve stem (111) co-axially slidable within a valve member (112), said valve member and valve stem defining an annular metering chamber (113), the metering valve further comprising outer and inner annular seals (117.118) operative between respective outer and inner ends of the valve member and the valve stem to seal the annular metering chamber therebetween, characterised in that the metering valve (110) comprises a layer of a clod plasma polymerised siloxane bonded to at least a portion of an internal surface of the valve member (112).
  • A particular embodiment of the present invention will now be described, by way of example only, with reference to the accompanying drawings, in which:
    • Figure 1 is a cross-sectional view through an inhaler; and
    • Figure 2 is a cross-sectional view of a metering valve according to the present invention.
  • In Figure 1, an inhaler 10 for a product such as a medicament comprises a housing 11 for receiving a pressurised dispensing container 12 of a medicament and a mouthpiece 14 for insertion into the mouth of a user of the inhaler 10.
  • The container housing 11 is generally cylindrical and open at its upper end. A lower wall 15 of the housing 11 includes an annular socket 16 for receiving the tubular valve stem 17 of the container 12. The socket 16 communicates via a duct 18 ending in an orifice 19 with the mouthpiece 14. The lower wall 15 also has holes 20 for allowing air to flow through the container housing 11 into the mouthpiece 14.
  • The mouthpiece 14 may be generally circular or shaped to fit the mouth and is connected to or forms a part of the housing 11.
  • In use, a patient or user holds the inhaler 10, usually in one hand, and apples his mouth to the mouth piece 14. The user then inhales through the mouthpiece 14 and this creates an airflow through the cylindrical housing 11, from its open end around the dispensing container 12, through the holes 20 and into the mouthpiece 14. After the user has started inhaling through the mouthpiece 14, the container 12 is depressed downwardly onto its stem 17 to release a dose of medicament from the container 12. The dose of medicament is projected by the pressure in the container 12 via the duct 18 and through the orifice 19. It then mixes with the airflow through the mouthpiece 14 and is hence inhaled by the user.
  • In traditional inhalers, all of the components are plastic mouldings, which gives rise to the deposition problems described above. The particular problem areas in devices such as inhalers are the internal surfaces 21 of the mouthpiece 14, the internal surfaces 22 of the duct 18 and the walls 23 defining the orifice 19. In some inhalers 10, the diameter of at least a part of the duct 18 can be as little as 0.5mm and so any deposition on its internal surfaces 22 could lead to not only the problem of a reduction in active drug components being available, but also dispensing difficulties.
  • The metering valve 110 illustrated in Figure 2 is another type of drug delivery device or dispenser, and includes a valve stem 111 which protrudes from and is axially slidable within a valve member 112, the valve member 112 and valve stem 111 defining therebetween an annular metering chamber 113. The valve member 112 is located within a valve body 114 which is positioned in a pressurised container (not shown) containing a product to be dispensed. The metering valve 110 is held in position with respect to the container by means of a ferrule 115 crimped to the top of the container and sealing being provided between the valve body 114 and container by an annular gasket 116.
  • An outer seal 117 and an inner seal 118 of an elastomeric material extend radially between the valve stem 111 and the valve member 112. The outer seal 117 is radially compressed between the valve member 112 and valve stem 111 so as to provide positive sealing contact, the compression being achieved by using a seal which provides an interference fit on the valve stem 111 and/or by the crimping of the ferrule 115 onto the pressurised container during assembly.
  • The valve stem 111 has an end 119 which protrudes from the valve member 112 and ferrule 115 which is a hollow tube and which is closed off by flange 120 which is located within the metering chamber 113. The hollow end 119 of valve stem 111 includes a discharge port 121 extending radially through the side wall of the valve stem 111. The valve stem 111 further has an intermediate section 122, which is also hollow and defining a central passage and which has a pair of spaced radial ports 123, 124 which are interconnected through a central cavity.
  • A spring 125 extends between a second flange 126, separating the intermediate section 122 of the valve stem 111 and an inner end 127 of the valve stem 111, and an end of the valve body 114 to bias the valve stem 111 in a non-dispensing position in which the first flange 120 is held in sealing contact with the outer seal 117. The second flange 126 is located outside the valve member 112, but within the valve body 114.
  • The metering chamber 113 is sealed from the atmosphere by the outer seal 117, and from the pressurised container to which the valve 110 is attached by the inner seal 118. In the illustration of the valve 110 shown in Figure 1 radial ports 123, 124, together with the central cavity in the intermediate section 122 of the valve member 111 connect the metering chamber 113 with the container so that in this non-dispensing condition the metering member 113 will be charged with product to be dispensed.
  • Upon depression of the valve stem 111 relative to the valve member 112 so that it moves inwardly into the container, the radial port 124 is closed off as it passes through the inner seal 118, thereby isolating the metering chamber 113 from the contents of the pressurised container. Upon further movement of the valve stem 111 in the same direction to a dispensing position the discharge port 121 passes through the outer seal 117 into communication with the metering chamber 113. In this dispensing position the product in the metering chamber 113 is free to be discharged to the atmosphere via the discharge port 121 and the cavity in the hollow end 119 of the valve stem 111.
  • When the valve stem 111 is released, the biasing of the return spring 125 causes the valve stem 111 to return to its original position. As a result the metering chamber 113 becomes recharged in readiness for further dispensing operations.
  • The component parts of the metering valve, such as valve members, and valve stems, are generally formed as single mouldings from material such as acetal, polyester or nylon which are prone to the deposition problems described above. Although in some cases it might be possible to include a separate liner of a material such as a fluoropolymer, ceramic or glass to line a portion of the area in which deposition problems occurs, this requires the re-design or modification of mouldings and mould tools so that the components can accommodate.such liners.
  • In the present invention we propose a solution in which the component parts of the drug dispensing devices are made by conventional tooling and moulds from the traditional materials listed above. They are then subjected to a cold plasma polymerisation treatment of one or more monomers which is a "hydrophobic" treatment which creates a very thin layer of the plasma polymer on the surface of the component parts which significantly reduces the deposition of active drugs on the relevant surfaces due to factors such as anti-frictional and waterproof characteristics and low surface energy.
  • The preferred monomers to use in this process are siloxanes, such as dimethyl siloxane, to give a layer of plasma polymerised dimethylsiloxane.
  • The process is known as "cold plasma" treatment as the temperature within the body of the plasma is ambient. Thus thermoplastic materials such as polybutyrene terephthalate (PBT), nylon, acetile and tetrabutyrene terephthalate (TBT) can be treated without fear of thermal damage. The treatment is a vacuum procedure in which the components are placed inside a chamber which is evacuated to less than 0.005 Torr. One or more monomers are introduced to the chamber at a controlled rate and a 13.56 MHZ r.f. signal is applied to an external antenna. The plasma is ignited within the chamber and maintained for a given time at the preselected power setting. At the end of the treatment the plasma is extinguished, the chamber flushed and the products retrieved. As a result a thin layer (for example 0.005 to 0.5 microns) of the plasma polymerised material is intimately bonded to the surface of the component.
  • Either an entire component within the drug delivery device, or just the surfaces of one or more component which would come into contact with the medicament during actuation, could be treated to provide an improved drug delivery device according to the present invention. In the metering valve of Figure 2, the valve member 112 alone may be treated. However, additional benefits can be achieved in treating some or all of the other plastic and rubber parts of the valve, including the valve body 114 and the seals 116, 117 and 118. Treatment of the seals 117 and 118 has the additional benefit that fiction between the seals 117 and 118 and valve stem 111 is reduced resulting in easier operation of the device. The level of friction between the valve stem 111 and seals 117 and 118 may be further reduced by treatment of the valve stem 111 itself. Such treatment reduces or eliminates the need for silicone emulsions or oils to be applied to the seals 117 and 118 and valve stem 111. Treatment of the seals 116, 117 and 118 also has the benefits of reducing levels of extractibles where the seals are manufactured from elastomeric materials, reducing the permeability of the seals to the propellant in the pressurised dispensing container and reducing the levels of absorption of product onto the surfaces of the seals. The method can also be used to treat components of many other delivery devices including nasal pumps, non-pressurised actuators, breath actuated inhaler devices and breath co-ordinating devices and so on.

Claims (5)

  1. A metering valve (110) for use with a pressurised dispensing container, the valve comprising a valve stem (111) co-axially slidable within a valve member (112), said valve member and valve stem defining an annular metering chamber (113), the metering valve further comprising outer and inner annular seals (117.118) operative between respective outer and inner ends of the valve member and the valve stem to seal the annular metering chamber therebetween, characterised in that the metering valve (110) comprises a layer of a cold plasma polymerised siloxane bonded to at least a portion of an internal surface of the valve member (112).
  2. A metering valve (110) as claimed in claim 1 in which the monomer for cold plasma polymerisation is dimethyl siloxane.
  3. A metering valve (110) as claimed in claim 1 or claim 2 in which the treated portion is made from a plastic polymer.
  4. A metering valve (110) as claimed in any preceding claim further comprising a layer of cold plasma polymerised siloxane bonded to a portion of the surface of the valve stem (111).
  5. A metering valve (110) as claimed in any preceding claim in which the valve further comprises a valve body (114) in which the valve member (112) is located, the valve body having a layer of cold plasma polymerised siloxane bonded to at least a portion of its surface.
EP01100963A 1998-02-23 1999-02-19 Drug delivery devices Expired - Lifetime EP1088567B1 (en)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
GBGB9803780.7A GB9803780D0 (en) 1998-02-23 1998-02-23 Improvements in or relating to metering valves for pressurised dispensing containers
GB9803780 1998-02-23
GBGB9808804.0A GB9808804D0 (en) 1998-04-24 1998-04-24 Improvements in drug delivery devices
GB9808804 1998-04-24
GBGB9814717.6A GB9814717D0 (en) 1998-02-23 1998-07-07 Improvements in drug delivery devices
GB9814717 1998-07-07
EP99905106A EP1066073B2 (en) 1998-02-23 1999-02-19 Pressurised dispensing containers

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
EP99905106A Division EP1066073B2 (en) 1998-02-23 1999-02-19 Pressurised dispensing containers

Publications (3)

Publication Number Publication Date
EP1088567A2 EP1088567A2 (en) 2001-04-04
EP1088567A3 EP1088567A3 (en) 2003-12-17
EP1088567B1 true EP1088567B1 (en) 2008-12-03

Family

ID=27269223

Family Applications (3)

Application Number Title Priority Date Filing Date
EP99905106A Expired - Lifetime EP1066073B2 (en) 1998-02-23 1999-02-19 Pressurised dispensing containers
EP01100963A Expired - Lifetime EP1088567B1 (en) 1998-02-23 1999-02-19 Drug delivery devices
EP02001152A Expired - Lifetime EP1208864B2 (en) 1998-02-23 1999-02-19 Improvements in drug delivery devices

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP99905106A Expired - Lifetime EP1066073B2 (en) 1998-02-23 1999-02-19 Pressurised dispensing containers

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP02001152A Expired - Lifetime EP1208864B2 (en) 1998-02-23 1999-02-19 Improvements in drug delivery devices

Country Status (28)

Country Link
EP (3) EP1066073B2 (en)
JP (3) JP2002503527A (en)
CN (1) CN1168510C (en)
AP (1) AP1264A (en)
AT (3) ATE415993T1 (en)
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AU742080B2 (en) 2001-12-20
EP1208864A3 (en) 2003-12-17
PT1208864E (en) 2007-07-02
DE69935681T2 (en) 2008-01-17
HK1036230A1 (en) 2001-12-28
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EP1066073B2 (en) 2008-02-27
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IS2506B (en) 2009-04-15
EP1208864B2 (en) 2012-06-06
MXPA00008174A (en) 2004-03-10
ID26130A (en) 2000-11-23
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NO20004196D0 (en) 2000-08-22
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HRP20000548A2 (en) 2001-08-31
ES2284733T5 (en) 2012-08-20
NO334842B1 (en) 2014-06-16
EE200000484A (en) 2001-08-15
SK286381B6 (en) 2008-08-05
TR200002439T2 (en) 2000-12-21
PL342515A1 (en) 2001-06-18
ATE415993T1 (en) 2008-12-15
DK1088567T3 (en) 2009-03-16
ES2284733T3 (en) 2007-11-16
CA2327046C (en) 2006-05-09
EP1088567A2 (en) 2001-04-04
DE69935681D1 (en) 2007-05-10
EA200000866A1 (en) 2001-04-23
EP1208864A2 (en) 2002-05-29
NO20004196L (en) 2000-08-22
DE69935681T3 (en) 2012-10-11
NZ506316A (en) 2003-11-28
DK1208864T4 (en) 2012-08-06
ATE357941T1 (en) 2007-04-15
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IL137650A0 (en) 2001-10-31
AP1264A (en) 2004-03-25
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JP2002503527A (en) 2002-02-05
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AU2540199A (en) 1999-09-06
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